Recalls distributed in Kansas
These notices name Kansas in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
2,850 stored notices name Kansas, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Kansas too — those are in the archive.
Reported Jul 17, 2013
ARO Pistachios, Pistachios raw kernel - no salt; Sold in 9 oz. raw kernel, no salt airtight jar; 2.5 lb raw Kernel, no…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ARO Pistachios, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 17, 2013
***REF C7120***APEX Arthroscopy Tubing Set. Intended for use for joint irrigation and dissention during arthroscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Linvatec Corp. dba ConMed Linvatec
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2013
Fudge Buttercream Frosted Peanut Butter cookies, some of which were mislabeled by being wrapped in Buttercream Frosted…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cheryls
FDA (openFDA food enforcement)
Reported Jul 10, 2013
1) VITROS 5,1 FS Chemistry System (product code 6801375) and 2) VITROS 5,1 FS Chemistry System Refurbished (product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2013
Computed Tomography X-ray systems Product Usage: The Brilliance CT 64, Ingenuity Core, and Ingenuity Core128 scanners…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 10, 2013
BASE, S-LIFT Instrument Case Product Usage: System cases are designed to hold and secure all instrumentation to be used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SpineFrontier, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2013
GE Healthcare Senographe Essential System. The Senographe 2000D system generates digital mamnmographic images that can…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2013
DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris MR Vital Signs Monitor: Product Usage: Monitor,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medrad Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2013
Brilliance CT 64, Ingenuity CT, Ingenuity Core, and Ingenuity Core128 scanners are whole body Computed Tomography X-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jun 26, 2013
Lightlife Farmer's Market Veggie Burgers, meat free, 12 oz/4-count bag, packaged in 5/12 oz-bag/cartons. Distributed…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Conagra Inc.
FDA (openFDA food enforcement)
Reported Jun 26, 2013
Echelon, Echelon Oval and Oasis MR imaging device systems; one unit per box. The Echelon, Echelon Oval and Oasis MR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Jun 26, 2013
GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5 reusable blades Product Usage: The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2013
Market Pantry, Sweet & Salty Mix, NET WT 3 oz (85g), UPC 0 85239 08131 0, INGREDIENTS: Peanuts (peanuts...) ...Honey…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Importing Co., Inc.
FDA (openFDA food enforcement)
Reported Jun 19, 2013
TX1 Tissue Removal System disposable handpieces. Product Usage: The TX1 Tissue Removal System is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Optisurgical Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2013
XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Atlantic Pro Nutrients, Inc. dba XYMOGEN
FDA (openFDA food enforcement)
Reported Jun 19, 2013
Blessing Brand Wild White EZ Peel Shrimp, 16/20 CT. 4 x 5 lbs cartons. The product is bagged in 5 lbs clear plastic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Blessing Seafood, Inc.
FDA (openFDA food enforcement)
Reported Jun 19, 2013
The product was originally distributed in a bulk container of 12/1 Dry Pints in boxes labeled "Karol" with the Lot No.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rio Queen Citrus, Inc.
FDA (openFDA food enforcement)
Reported Jun 19, 2013
"Shurfine CREAMERY SELECT PREMIUM ICE CREAM Dulce de Leche Caramel Swirled in Caramel Ice Cream KEEP FROZEN 1.75 QUARTS…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Southwest Ice Cream Specialties
FDA (openFDA food enforcement)
Reported Jun 12, 2013
FAST Procedure Kit. Intended for use as a Minor Surgical Procedures Tray.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Optisurgical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2013
REF 8229705 x1 NIM TriVantage EMG Endotracheal Tube 5.0 mm I.D. x 6.5 mm O.D. Medtronic Xomed, Inc., 6743 Southpoint…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Xomed, Inc.
FDA (openFDA device enforcement)
Reported Jun 12, 2013
BrightView SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jun 5, 2013
EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nephron Pharmaceuticals Corp.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2013
Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Plunger Delivery System, 4", Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthovita, Inc., dba Stryker Orthobiologics.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2013
***REF S-3D*** 3mm Diamond Ball. Used for cutting and shaping bone.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.